1. Expression of the vHNF1/HNF1β homeoprotein gene during mouse organogenesis;Coffinier;Mech Dev,1999
2. Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study;Weber;J Am Soc Nephrol,2006
3. HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort;Thomas;Pediatr Nephrol,2011
4. Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes;Madariaga;Clin J Am Soc Nephrol,2013
5. HNF1B mutations associate with hypomagnesemia and renal magnesium wasting;Adalat;J Am Soc Nephrol,2009